首页> 美国卫生研究院文献>The Journal of Biophysical and Biochemical Cytology >SCAR knockouts in Dictyostelium: WASP assumesSCAR’s position and upstream regulators in pseudopods
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SCAR knockouts in Dictyostelium: WASP assumesSCAR’s position and upstream regulators in pseudopods

机译:WASP假设在网柄菌属中有SCAR基因敲除SCAR在伪足中的位置和上游调节器

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摘要

Under normal conditions, the Arp2/3 complex activator SCAR/WAVE controls actin polymerization in pseudopods, whereas Wiskott–Aldrich syndrome protein (WASP) assembles actin at clathrin-coated pits. We show that, unexpectedly, Dictyostelium discoideum SCAR knockouts could still spread, migrate, and chemotax using pseudopods driven by the Arp2/3 complex. In the absence of SCAR, some WASP relocated from the coated pits to the leading edge, where it behaved with similar dynamics to normal SCAR, forming split pseudopods and traveling waves. Pseudopods colocalized with active Rac, whether driven by WASP or SCAR, though Rac was activated to a higher level in SCAR mutants. Members of the SCAR regulatory complex, in particular PIR121, were not required for WASP regulation. We thus show that WASP is able to respond to all core upstream signals and that regulators coupled through the other members of SCAR’s regulatory complex are not essential for pseudopod formation. We conclude that WASP and SCAR can regulate pseudopod actin using similar mechanisms.
机译:在正常情况下,Arp2 / 3复合激活物SCAR / WAVE控制假足中的肌动蛋白聚合,而Wiskott-Aldrich综合征蛋白(WASP)在网格蛋白包被的小孔处组装肌动蛋白。我们表明,出乎意料的是,使用Arp2 / 3复合物驱动的假足,盘基网柄菌SCAR基因敲除仍然可以传播,迁移和趋化。在没有SCAR的情况下,一些WASP从涂层的凹坑移至前缘,其行为与普通SCAR相似,形成了伪足和行波。伪足与活性Rac共定位,无论是由WASP还是SCAR驱动,尽管Rac在SCAR突变体中被激活到更高的水平。 WASP法规不需要SCAR法规综合体的成员,尤其是PIR121。因此,我们表明WASP能够响应所有核心上游信号,并且通过SCAR监管机构的其他成员耦合的监管机构对于伪足的形成并不是必不可少的。我们得出的结论是,WASP和SCAR可以使用类似的机制调节假足肌动蛋白。

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